Angalena, R <br/><br/>
A novel homozygous point mutation at codon 82 (HBB:c.247A > T) in the beta-globin gene leads to thalassemia major.  [electronic resource] 

 -  International journal of laboratory hematology  Oct 2010 
 - 548-9 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1751-553X 
<br/><br/><label>Standard No.: </label>10.1111/j.1751-553X.2009.01217.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Female<br/>Homozygote<br/>Humans<br/>Point Mutation<br/>beta-Globins--genetics<br/>beta-Thalassemia--genetics